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Journal of Clinical Immunology|February 13, 2020
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical ClassificationAziz Bousfiha, Leila Jeddane, Capucine Picard, et al.
Journal of Clinical Immunology|May 19, 2016
Hyper IgM Syndrome: a Report from the USIDNET RegistryEmily A Leven, Patrick Maffucci, Hans D Ochs, et al.
Clinical Immunology (Orlando, Fla.)|January 10, 2002
Progressive neurodegeneration in patients with primary immunodeficiency disease on IVIG treatmentUlrike H M Ziegner, Roger H Kobayashi, Charlotte Cunningham-Rundles, et al.
Journal of Clinical Immunology|August 20, 2020
A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody DeficiencyHye Sun Kuehn, Andrea Bernasconi, Julie E Niemela, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2018
Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysisPatrick Maffucci, Benedetta Bigio, Franck Rapaport, et al.
Journal of Clinical Immunology|September 9, 2020
Correction to: A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody DeficiencyHye Sun Kuehn, Andrea Bernasconi, Julie E Niemela, et al.
The Journal of Allergy and Clinical Immunology|November 8, 2017
Ruxolitinib partially reverses functional natural killer cell deficiency in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutationsAlexander Vargas-Hernández, Emily M Mace, Ofer Zimmerman, et al.
The Journal of Allergy and Clinical Immunology|June 24, 2018
Patients with common variable immunodeficiency with autoimmune cytopenias exhibit hyperplastic yet inefficient germinal center responsesNeil Romberg, Carole Le Coz, Salomé Glauzy, et al.
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